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EAAT2 antibody extracellular domain - 250 203 K.O.

EAATs are transmembrane proteins involved in the removal of extracellular glutamate
Rabbit polyclonal purified antibody
Cat. No.: 250 203
Amount: 50 µg
Price: $380.00
Cat. No. 250 203 50 µg specific antibody, lyophilized. Affinity purified with the immunogen. Albumin and azide were added for stabilization. For reconstitution add 50 µl H2O to get a 1mg/ml solution in PBS. Then aliquot and store at -20°C to -80°C until use.
Antibodies should be stored at +4°C when still lyophilized. Do not freeze!
Applications
 
WB: 1 : 1000 (AP staining) gallery  
IP: not tested yet
ICC: not tested yet
IHC: 1 : 1000 up to 1 : 2000 gallery  
IHC-P: 1 : 500 gallery  
Immunogen Synthetic peptide corresponding to AA 146 to 161 from mouse EAAT2 (UniProt Id: P43006)
Reactivity Reacts with: human (P43004), rat (P31596), mouse (P43006).
Other species not tested yet.
Specificity K.O. validated
Matching control protein/peptide 250-2P
Data sheet 250_203.pdf

References for EAAT2 - 250 203

Rapid recycling of glutamate transporters on the astroglial surface.
Michaluk P, Heller JP, Rusakov DA
eLife (2021) 10: . 250 203 WB; tested species: mouse
Astrocyte dysfunction increases cortical dendritic excitability and promotes cranial pain in familial migraine.
Romanos J, Benke D, Pietrobon D, Zeilhofer HU, Santello M
Science advances (2020) 623: eaaz1584. 250 203 WB; tested species: mouse
Differences in glutamate uptake between cortical regions impact neuronal NMDA receptor activation.
Romanos J, Benke D, Saab AS, Zeilhofer HU, Santello M
Communications biology (2019) 2: 127. 250 203 WB; tested species: mouse
Chronic Toxoplasma infection is associated with distinct alterations in the synaptic protein composition.
Lang D, Schott BH, van Ham M, Morton L, Kulikovskaja L, Herrera-Molina R, Pielot R, Klawonn F, Montag D, Jänsch L, Gundelfinger ED, et al.
Journal of neuroinflammation (2018) 151: 216. 250 203 WB, IHC; tested species: mouse
Strategies for immunohistochemical protein localization using antibodies: What did we learn from neurotransmitter transporters in glial cells and neurons.
Danbolt NC, Zhou Y, Furness DN, Holmseth S
Glia (2016) 6412: 2045-2064. 250 203 WB
Region-specific changes in gene expression are associated with cognitive deficits in the alpha-synuclein-induced model of Parkinson's disease: A transcriptomic profiling study.
Manchinu MF, Pala M, Palmas MF, Diana MA, Maschio A, Etzi M, Pisanu A, Diana FI, Marongiu J, Mansueto S, Carboni E, et al.
Experimental neurology (2024) 372: 114651. 250 203 IHC; tested species: rat
Glutamate transporters EAAT2 and EAAT5 differentially shape synaptic transmission from rod bipolar cell terminals.
Tang FS, Yuan HL, Liu JB, Zhang G, Chen SY, Ke JB
eNeuro (2022) : . 250 203 IHC; tested species: mouse
Glioblastoma hijacks neuronal mechanisms for brain invasion.
Venkataramani V, Yang Y, Schubert MC, Reyhan E, Tetzlaff SK, Wißmann N, Botz M, Soyka SJ, Beretta CA, Pramatarov RL, Fankhauser L, et al.
Cell (2022) : . 250 203 IHC; tested species: mouse
Chronic Toxoplasma infection is associated with distinct alterations in the synaptic protein composition.
Lang D, Schott BH, van Ham M, Morton L, Kulikovskaja L, Herrera-Molina R, Pielot R, Klawonn F, Montag D, Jänsch L, Gundelfinger ED, et al.
Journal of neuroinflammation (2018) 151: 216. 250 203 WB, IHC; tested species: mouse
Characterization of Tissue Plasminogen Activator Expression and Trafficking in the Adult Murine Brain.
Stevenson TK, Lawrence DA
eNeuro () 54: . 250 203 IHC; tested species: mouse
Pentylenetetrazole-induced Seizure Susceptibility in the Tau58/4 Transgenic Mouse Model of Tauopathy.
Van Erum J, Valkenburg F, Van Dam D, Paul De Deyn P
Neuroscience (2019) : . 250 203 IHC-P; tested species: mouse
Crym-positive striatal astrocytes gate perseverative behaviour.
Ollivier M, Soto JS, Linker KE, Moye SL, Jami-Alahmadi Y, Jones AE, Divakaruni AS, Kawaguchi R, Wohlschlegel JA, Khakh BS
Nature (2024) : . 250 203 IHC-Fr; tested species: mouse
Cat. No.: 250 203
Amount: 50 µg
Price: $380.00
Rapid recycling of glutamate transporters on the astroglial surface.
Michaluk P, Heller JP, Rusakov DA
eLife (2021) 10: . 250 203 WB; tested species: mouse
Astrocyte dysfunction increases cortical dendritic excitability and promotes cranial pain in familial migraine.
Romanos J, Benke D, Pietrobon D, Zeilhofer HU, Santello M
Science advances (2020) 623: eaaz1584. 250 203 WB; tested species: mouse
Differences in glutamate uptake between cortical regions impact neuronal NMDA receptor activation.
Romanos J, Benke D, Saab AS, Zeilhofer HU, Santello M
Communications biology (2019) 2: 127. 250 203 WB; tested species: mouse
Chronic Toxoplasma infection is associated with distinct alterations in the synaptic protein composition.
Lang D, Schott BH, van Ham M, Morton L, Kulikovskaja L, Herrera-Molina R, Pielot R, Klawonn F, Montag D, Jänsch L, Gundelfinger ED, et al.
Journal of neuroinflammation (2018) 151: 216. 250 203 WB, IHC; tested species: mouse
Strategies for immunohistochemical protein localization using antibodies: What did we learn from neurotransmitter transporters in glial cells and neurons.
Danbolt NC, Zhou Y, Furness DN, Holmseth S
Glia (2016) 6412: 2045-2064. 250 203 WB
Region-specific changes in gene expression are associated with cognitive deficits in the alpha-synuclein-induced model of Parkinson's disease: A transcriptomic profiling study.
Manchinu MF, Pala M, Palmas MF, Diana MA, Maschio A, Etzi M, Pisanu A, Diana FI, Marongiu J, Mansueto S, Carboni E, et al.
Experimental neurology (2024) 372: 114651. 250 203 IHC; tested species: rat
Glutamate transporters EAAT2 and EAAT5 differentially shape synaptic transmission from rod bipolar cell terminals.
Tang FS, Yuan HL, Liu JB, Zhang G, Chen SY, Ke JB
eNeuro (2022) : . 250 203 IHC; tested species: mouse
Glioblastoma hijacks neuronal mechanisms for brain invasion.
Venkataramani V, Yang Y, Schubert MC, Reyhan E, Tetzlaff SK, Wißmann N, Botz M, Soyka SJ, Beretta CA, Pramatarov RL, Fankhauser L, et al.
Cell (2022) : . 250 203 IHC; tested species: mouse
Chronic Toxoplasma infection is associated with distinct alterations in the synaptic protein composition.
Lang D, Schott BH, van Ham M, Morton L, Kulikovskaja L, Herrera-Molina R, Pielot R, Klawonn F, Montag D, Jänsch L, Gundelfinger ED, et al.
Journal of neuroinflammation (2018) 151: 216. 250 203 WB, IHC; tested species: mouse
Characterization of Tissue Plasminogen Activator Expression and Trafficking in the Adult Murine Brain.
Stevenson TK, Lawrence DA
eNeuro () 54: . 250 203 IHC; tested species: mouse
Pentylenetetrazole-induced Seizure Susceptibility in the Tau58/4 Transgenic Mouse Model of Tauopathy.
Van Erum J, Valkenburg F, Van Dam D, Paul De Deyn P
Neuroscience (2019) : . 250 203 IHC-P; tested species: mouse
Crym-positive striatal astrocytes gate perseverative behaviour.
Ollivier M, Soto JS, Linker KE, Moye SL, Jami-Alahmadi Y, Jones AE, Divakaruni AS, Kawaguchi R, Wohlschlegel JA, Khakh BS
Nature (2024) : . 250 203 IHC-Fr; tested species: mouse
WB
IHC
IHC-P
Background
Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system. After the release of glutamate from synaptic vesicles into the synaptic cleft during neurotransmission, excitatory amino acid transporters (EAATs) remove extracellular glutamate to avoid excitotoxic levels.
Five EAATs with differential expression patterns have been described so far: EAAT 1, also referred to as GLAST and SLC1A3, has neuroprotective potential following ischemia and is expressed by reactive astrocytes and activated microglia. EAAT 2 (GLT-1, SLC1A2) is the most abundant and primarily expressed in astrocytes. EAAT 3 / SLC1A1 is expressed in neurons and has also been shown to be involved in the uptake of extracelluar cysteine. EAAT 4 shows weak expression in the forebrain and high levels in Purkinje cells of the cerebellum. EAAT 5 has only been described for humans and is primarily expressed in the retina.
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